Canonical Allele Identifier: CA350827618

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197396
• MyVariant Identifiers: chr2:g.225368498C>A (hg19) ; chr2:g.224503781C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503781C>A , CM000664.2:g.224503781C>A	GRCh38
NC_000002.11:g.225368498C>A , CM000664.1:g.225368498C>A	GRCh37
NC_000002.10:g.225076742C>A	NCBI36
NG_032169.1:g.86617G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1248G>T MANE Select	ENSP00000264414.4:p.Met416Ile
ENST00000264414.8:c.1248G>T	ENSP00000264414.4:p.Met416Ile
ENST00000344951.8:c.1050G>T	ENSP00000343601.4:p.Met350Ile
ENST00000409096.5:c.1176G>T	ENSP00000387200.1:p.Met392Ile
ENST00000409777.5:c.1176G>T	ENSP00000386525.1:p.Met392Ile
ENST00000481135.1:n.544G>T
ENST00000617432.4:c.-29G>T	ENSP00000477851.1:n.-29G>T
NM_001257197.1:c.1050G>T	NP_001244126.1:p.Met350Ile
NM_001257198.1:c.1266G>T	NP_001244127.1:p.Met422Ile
NM_003590.4:c.1248G>T	NP_003581.1:p.Met416Ile
XM_006712800.2:c.1215G>T	XP_006712863.2:p.Met405Ile
XM_011511994.1:c.1101G>T	XP_011510296.1:p.Met367Ile
XM_011511995.1:c.1206G>T	XP_011510297.1:p.Met402Ile
XM_011511996.1:c.1056G>T	XP_011510298.1:p.Met352Ile
XM_011511997.1:c.948G>T	XP_011510299.1:p.Met316Ile
XM_011511994.3:c.1101G>T	XP_011510296.1:p.Met367Ile
XM_011511996.2:c.1056G>T	XP_011510298.1:p.Met352Ile
NM_003590.5:c.1248G>T MANE Select	NP_003581.1:p.Met416Ile
NM_001257198.2:c.1266G>T	NP_001244127.1:p.Met422Ile
NM_001257197.2:c.1050G>T	NP_001244126.1:p.Met350Ile